2. Gene
  3. PNCK - pregnancy up-regulated nonubiquitous CaM kinase Gene

PNCK - pregnancy up-regulated nonubiquitous CaM kinase Gene

  • Gene
  • Protein
  • Disease
  • Agent
  • Ortholog
Homo sapiens

Also known as BSTK3; CaMK1b

Gene ID: 139728 | Gene type: protein coding

About PNCK

Cytogenetic location: Xq28 Genomic coordinates (GRCh38): X:153,669,733-153,687,771 (from NCBI)

This gene has 32 transcripts (splice variants), 102 orthologues and 22 paralogues. Biased expression in brain (RPKM 7.4), prostate (RPKM 4.6) and 11 other tissues.

Summary

PNCK is a member of the calcium/calmodulin-dependent protein kinase family of protein serine/threonine kinases (see CAMK1; MIM 604998) (Gardner et al., 2000 [PubMed 10673339]).[supplied by OMIM, Mar 2008]

PNCK Products(8)

mRNA Protein Name
NM_001039582.3 NP_001034671.3 calcium/calmodulin-dependent protein kinase type 1B isoform a
NM_001135740.2 NP_001129212.1 calcium/calmodulin-dependent protein kinase type 1B isoform b
NM_001366975.1 NP_001353904.1 calcium/calmodulin-dependent protein kinase type 1B isoform c
NM_001366976.1 NP_001353905.1 calcium/calmodulin-dependent protein kinase type 1B isoform c
NM_001366977.1 NP_001353906.1 calcium/calmodulin-dependent protein kinase type 1B isoform c
NM_001366978.1 NP_001353907.1 calcium/calmodulin-dependent protein kinase type 1B isoform c
NM_001366979.1 NP_001353908.1 calcium/calmodulin-dependent protein kinase type 1B isoform c
NM_001366980.1 NP_001353909.1 calcium/calmodulin-dependent protein kinase type 1B isoform c

PNCK Protein Structure

Pkinase

Pkinase: Protein kinase domain (15 - 270)

  • 0
  • 100
  • 200
  • 300
  • 343 a.a.
Protein Preferred Names Protein Names

calcium/calmodulin-dependent protein kinase type 1B

caM kinase I beta

Related Diseases

Diseases Alias
Syndromic X-Linked Intellectual Disability Lubs Type

Lubs X-Linked Mental Retardation Syndrome

Mecp2 Duplication Syndrome

Mental Retardation, X-Linked, Syndromic, Lubs Type

Mental Retardation, X-Linked, With Recurrent Respiratory Infections

Mrxsl

X-Linked Intellectual Disability-Hypotonia-Recurrent Infections Syndrome

Mental Retardation, X-Linked Syndromic, Lubs Type
Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Related Agents

Pre-clinical Phase
Bioactive Molecules (1)
Cat. No. Product Name Effect
Purity Rare Diseases
HY-RS10775 PNCK Human Pre-designed siRNA Set A Pre-designed Sets / Unkown

Orthologs Information

Species Symbol Source ID
Bos taurus PNCK VGNC VGNC:33079
Mus musculus PNCK MGD MGI:1347357
Macaca mulatta PNCK VGNC VGNC:76020
Canis familiaris PNCK VGNC VGNC:44740
Felis catus PNCK VGNC VGNC:64258
Rattus norvegicus PNCK RGD RGD:69249
Others PNCK NCBI